Here, we describe the recent progress toward construction of 1-azabicyclic structures using
a domino hydroformylation double cyclization strategy of an amide bearing the trisubstituted …

A domino method for the rapid syntheses of 1‐azabicyclo [xy 0] alkane scaffolds, such as
indolizidines, quinolizidines, decahydropyridoazepines, and their derivatives, has been …

A stereodivergent approach toward total syntheses of Dendrobatid alkaloids 223A and 6-epi-
223A is described. The approach features a concise construction of an indolizidine skeleton …

Hydroformylation of Homoallylic Azides: A Rapid Approach toward Alkaloids | Organic Letters
ACS ACS Publications C&EN CAS Find my institution Log In Organic Letters ACS Publications …

Herein, we report a fully atom-economic and highly step-economic cascade dearomatization
with non-activated phenyl and other hetero-aryl rings for access to aniline-tethered spiro …

Synthetic strategies are one of the most critical factors for the success of a synthetic
campaign, but most importantly they are crucial for the economy and the efficiency of the …

A novel domino reaction, alkyne-mediated domino hydroformylation/double cyclization, has
been developed for rapid preparation of indolizidine type alkaloids. DFT calculations were …

A parallel, versatile and efficient route to synthesis of pyrrolidinoindoline and
tetrahydrofuranoindoline alkaloids from cinnamyl derivatives has been developed, featuring …

Tetrahydrocarbazole is the central core for several biologically active alkaloids, and
regioselective synthesis of this core is a challenging task. Herein, we report an efficient …

A catalytic two-step reaction sequence was developed to access a range of complex
heterocyclic frameworks based on biorelevant indole/oxindole scaffolds. The reaction …